Endocrine Flashcards

1
Q

Most common presenting complaint to pediatric endocrinologist

A

growth disturbances

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2
Q

fetal growth dependent on

A

maternal factors

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3
Q

late infancy growth dependent on

A

GH/IGF-1 axis and thyroid hormone

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4
Q

pubertal growth dependent on

A

sex hormones as well as GH/IGF-1 axis and the thyroid gland

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5
Q

define short stature

A

height less than 3% on growth chart

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6
Q

endocrine causes of short stature

A

growth hormone deficiency or resistance
hypothyroid
diabetes mellitus

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7
Q

Decreased growth velocity, delay in skeletal maturation. Short stature (below 5th percentile), grows normally for first year but drops off during the 2nd. Height may be more retarded than weight

A

growth hormone deficiency

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8
Q

most common form of growth hormone deficiency

A

idiopathic

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9
Q

treat GH deficiency

A
correct underlying disease
replace GH (only for FDA approved conditions
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10
Q

what do you worry about with excessive GH secretion (rare)

A

pituitary adenoma

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11
Q

most common cause of hypothyroid in childhood. Most common cause of goiter and thyroiditis

A

Hashimotos thyroiditis (autoimmune thyroiditis)

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12
Q

most common neonatal metabolic disorder

A

congenital hypothyroid

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13
Q

treat hashimoto

A

levothyroxine (not if euthyroid)

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14
Q

who has increased incidence of hashimoto

A

trisomy 21, turners

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15
Q

physical and mental sluggishness, pale, gray, cool mottled skin. Non pitting edema, constipation, large tongue, poor muscle tone, lordosis, bradycardia, hoarse cry or voice, skin dry, coarse, scaly, yellowish. Lateral thinning of eyebrows

A

hypothyroid

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16
Q

most common cause of hyperthyroidism in kids

A

graves

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17
Q

nervousness, emotional lability, hyperactivity, weight loss. Insomnia, personality changes, diarrhea ,palpitations, heat intolerance,tremor, increased sweating

A

hyperthyroid (graves)

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18
Q

labs for graves

A

TSH low

FT4, T3, T4 elevated

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19
Q

labs for hashimoto

A

T3, T4, and FT4 decreased. TSH elevated

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20
Q

treat hyperthyroid

A

beta blocker, antithyroid meds (PTU, methimazole)

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21
Q

this is more common in girls. Younger than 8 years old

A

precocious puberty (central idiopathic precocity)

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22
Q

central precocious puberty

A
CNS abnormality (tumor)
familial
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23
Q

peripheral precocious puberty

A

ovarian cyst, adrenal tumors, CAH

24
Q

adrenarche – pubic hair, axillary hair, acnea, some increased body odor

A

adrenal tumor

25
Symptoms of estrogen excess – breast development and vaginal bleeding
ovarian cysts or tumors
26
treat central precocious puberty
GnRH analog- Leuprolide
27
boys- pseudoprecocious puberty
peripheral stimulation, GnRH independent, small testes
28
boys- true precocious puberty
central stimulation, GnRH dependent, large testes
29
define delayed puberty in boys and girls
boys 14 no signs, girls 13 no signs
30
primary hypogonadism
absence / malfunction/ destruction of ovarian or testicular tissue
31
central hypogonadism
pituitary or hypothalamic dysfunction (panhypopituitarism, CNS tumor, gonadotropin deficiency)
32
most common cause of delayed puberty in boys
Kleinfelter syndrome
33
labs for primary vs central hypogonadism
primary: LH, FSH elevated central: LH, FSH low
34
treat hypogonadism
sex steroid replacement
35
most common cause of female virilization, pseudohermaphrodite
CAH
36
most frequent cause of ambiguous genitalia in the newborn
CAH
37
labs for CAH
elevated 17 OH, deficiency of 21 hydroxylase, electrolyte imbalances
38
treat CAH
hydrocortisone, mineralcorticoid
39
most common etiology of CAH
deficiency of 21 hydrocylase
40
adrenal insufficiency
uncommon CAH autoimmune destruction (Addisons)
41
adrenal excess
uncommon, Cushings | Exogenous steroids most common cause of cushings in children
42
test for adrenal insufficiency
ACTH stim test
43
treat adrenal insufficiency
replace hydrocortisone, fludrocortisone
44
Truncal adoposity with thin extremities, moon facies, muscle wasting, weakness, easy bruising, purplish striae HTN, osteoporosis, glycosuria, hyperglycemia
Cushing's syndrome
45
test for cushings
urinary cortisol level | dexamethasone suppression test
46
type I DM
insulin dependent, juvenile diabetes or IDDM
47
most common type of DM in children
type I (this is almost not true anymore)
48
what other endocrine system would you check in a kid with type I DM
thyroid (hypothyroid can be associated)
49
treat type I DM
insulin, diet,exercise, stress management, glucose monitoring
50
triad type I DM
polyuria polydipsia polyphagia
51
ancanthosis nigricans
changes in skin related to type II DM
52
type II DM
“Non-insulin dependent” – insulin resistance and insulin insensitivity
53
type II DM has an association with this syndrome
polycystic ovarian syndrome
54
what do children die from in DKA
cerebral edema
55
ketone effect on serum pH
lower (the produce free hydrogen ions)
56
treat DKA
replace fluid insulin replace body salts correct acidosis